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In January 2026, the FDA told drugmakers to strip suicide-warning language from Wegovy, Zepbound and Saxenda labels
Federal drug regulators concluded that three obesity medicines should no longer carry label language warning about suicidal ...
Add Yahoo as a preferred source to see more of our stories on Google. The U.S. Food and Drug Administration (FDA) wants to make them easier to read. On Tuesday, the agency proposed a new rule ...
Add Yahoo as a preferred source to see more of our stories on Google. The guide helps global food and packaging stakeholders better understand regulatory The US Food and Drug Administration (FDA) ...
The U.S. Food and Drug Administration announced it will now be requiring updated safety labels for all opioid pain medications to better highlight the risks of long-term use, including misuse, ...
The US Food and Drug Administration (FDA) on Tuesday announced class-wide safety labeling changes for immediate-release (IR) opioid pain medications, which make up about 90% of all opioid ...
The Food and Drug Administration (FDA) is considering placing a black-box warning on antidepressant use in pregnancy, alarming some doctors who worry that a reignited debate about the drugs’ safety ...
New Age Meats creates plant-based meat alternatives for traditional pork products by utilizing a combination of plant-based ingredients and cultivated pork. Source: New Age Meats Draft guidance ...
The FDA recently issued a final rule, which updates the definition for the implied nutrient content claim “healthy.” The definition change aims for “healthy” to be consistent with current nutrition ...
The US Food and Drug Administration (FDA) on Friday released draft guidance describing the process for drug companies when they have to update a generic’s label after the reference product (for which ...
The US Food and Drug Administration is proposing that nutrition information be placed on the front of packaged foods to provide at-a-glance information about saturated fat, sodium and added sugar.
Federal law requires every prescription drug to include a document describing dosing guidelines, contraindications, results from clinical trials and safety considerations. But a spate of recent court ...
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